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      Identifying the critical state of complex biological systems by the directed-network rank score method

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      , , , ,
      Bioinformatics
      Oxford University Press

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          Abstract

          Motivation

          Catastrophic transitions are ubiquitous in the dynamic progression of complex biological systems; that is, a critical transition at which complex systems suddenly shift from one stable state to another occurs. Identifying such a critical point or tipping point is essential for revealing the underlying mechanism of complex biological systems. However, it is difficult to identify the tipping point since few significant differences in the critical state are detected in terms of traditional static measurements.

          Results

          In this study, by exploring the dynamic changes in gene cooperative effects between the before-transition and critical states, we presented a model-free approach, the directed-network rank score (DNRS), to detect the early-warning signal of critical transition in complex biological systems. The proposed method is applicable to both bulk and single-cell RNA-sequencing (scRNA-seq) data. This computational method was validated by the successful identification of the critical or pre-transition state for both simulated and six real datasets, including three scRNA-seq datasets of embryonic development and three tumor datasets. In addition, the functional and pathway enrichment analyses suggested that the corresponding DNRS signaling biomarkers were involved in key biological processes.

          Availability and implementation

          The source code is freely available at https://github.com/zhongjiayuan/DNRS.

          Supplementary information

          Supplementary data are available at Bioinformatics online.

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          Most cited references50

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          clusterProfiler: an R package for comparing biological themes among gene clusters.

          Increasing quantitative data generated from transcriptomics and proteomics require integrative strategies for analysis. Here, we present an R package, clusterProfiler that automates the process of biological-term classification and the enrichment analysis of gene clusters. The analysis module and visualization module were combined into a reusable workflow. Currently, clusterProfiler supports three species, including humans, mice, and yeast. Methods provided in this package can be easily extended to other species and ontologies. The clusterProfiler package is released under Artistic-2.0 License within Bioconductor project. The source code and vignette are freely available at http://bioconductor.org/packages/release/bioc/html/clusterProfiler.html.
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            Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources.

            DAVID bioinformatics resources consists of an integrated biological knowledgebase and analytic tools aimed at systematically extracting biological meaning from large gene/protein lists. This protocol explains how to use DAVID, a high-throughput and integrated data-mining environment, to analyze gene lists derived from high-throughput genomic experiments. The procedure first requires uploading a gene list containing any number of common gene identifiers followed by analysis using one or more text and pathway-mining tools such as gene functional classification, functional annotation chart or clustering and functional annotation table. By following this protocol, investigators are able to gain an in-depth understanding of the biological themes in lists of genes that are enriched in genome-scale studies.
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              Metascape provides a biologist-oriented resource for the analysis of systems-level datasets

              A critical component in the interpretation of systems-level studies is the inference of enriched biological pathways and protein complexes contained within OMICs datasets. Successful analysis requires the integration of a broad set of current biological databases and the application of a robust analytical pipeline to produce readily interpretable results. Metascape is a web-based portal designed to provide a comprehensive gene list annotation and analysis resource for experimental biologists. In terms of design features, Metascape combines functional enrichment, interactome analysis, gene annotation, and membership search to leverage over 40 independent knowledgebases within one integrated portal. Additionally, it facilitates comparative analyses of datasets across multiple independent and orthogonal experiments. Metascape provides a significantly simplified user experience through a one-click Express Analysis interface to generate interpretable outputs. Taken together, Metascape is an effective and efficient tool for experimental biologists to comprehensively analyze and interpret OMICs-based studies in the big data era.
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                Author and article information

                Contributors
                Role: Associate Editor
                Journal
                Bioinformatics
                Bioinformatics
                bioinformatics
                Bioinformatics
                Oxford University Press
                1367-4803
                1367-4811
                15 December 2022
                25 October 2022
                25 October 2022
                : 38
                : 24
                : 5398-5405
                Affiliations
                School of Mathematics and Big Data, Foshan University , Foshan 528000, China
                School of Mathematics, South China University of Technology , Guangzhou 510640, China
                School of Biology and Biological Engineering, South China University of Technology , Guangzhou 510640, China
                School of Mathematics, South China University of Technology , Guangzhou 510640, China
                School of Mathematics, South China University of Technology , Guangzhou 510640, China
                School of Mathematics, South China University of Technology , Guangzhou 510640, China
                Pazhou Lab , Guangzhou 510330, China
                Author notes

                The authors wish it to be known that, in their opinion, Jiayuan Zhong and Chongyin Han should be regarded as Joint First Authors.

                To whom correspondence should be addressed. Email: scliurui@ 123456scut.edu.cn or chenpei@ 123456scut.edu.cn
                Author information
                https://orcid.org/0000-0003-0508-1383
                https://orcid.org/0000-0002-2017-576X
                https://orcid.org/0000-0002-4547-8695
                Article
                btac707
                10.1093/bioinformatics/btac707
                9750123
                36282843
                94cc60e0-482f-4e2c-be34-093c06db75e6
                © The Author(s) 2022. Published by Oxford University Press.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 27 June 2022
                : 21 September 2022
                : 15 October 2022
                : 24 October 2022
                : 09 November 2022
                Page count
                Pages: 8
                Funding
                Funded by: National Natural Science Foundation of China, DOI 10.13039/501100001809;
                Award ID: 12026608
                Award ID: 62172164
                Award ID: 12271180
                Award ID: 12131020
                Funded by: Guangdong Basic and Applied Basic Research Foundation, DOI 10.13039/501100021171;
                Award ID: 2019B151502062
                Funded by: Guangdong Provincial Key Laboratory of Human Digital Twin;
                Award ID: 2022B1212010004
                Categories
                Original Paper
                Systems Biology
                AcademicSubjects/SCI01060

                Bioinformatics & Computational biology
                Bioinformatics & Computational biology

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